rs55680580
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs55680580(A;A) |
Make rs55680580(A;T) |
Make rs55680580(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 290578 |
is a | snp |
is | mentioned by |
dbSNP | rs55680580 |
dbSNP (classic) | rs55680580 |
ClinGen | rs55680580 |
ebi | rs55680580 |
HLI | rs55680580 |
Exac | rs55680580 |
Gnomad | rs55680580 |
Varsome | rs55680580 |
LitVar | rs55680580 |
Map | rs55680580 |
PheGenI | rs55680580 |
Biobank | rs55680580 |
1000 genomes | rs55680580 |
hgdp | rs55680580 |
ensembl | rs55680580 |
geneview | rs55680580 |
scholar | rs55680580 |
rs55680580 | |
pharmgkb | rs55680580 |
gwascentral | rs55680580 |
openSNP | rs55680580 |
23andMe | rs55680580 |
SNPshot | rs55680580 |
SNPdbe | rs55680580 |
MSV3d | rs55680580 |
GWAS Ctlg | rs55680580 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 24159190] |
Trait | Serum dimethylarginine levels (symmetric) |
Title | Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality. |
Risk Allele | A |
P-val | 8E-6 |
Odds Ratio | .29 [0.16-0.42] unit increase |